Calcined Co-chelating, imine-crosslinking chitosan as the ORR catalyst of an anion exchange membrane fuel cell

IF 3.1 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Yen-Zen Wang , Ko-Shan Ho , Yu-Chang Huang , Yu-Wei Cheng , Chia-Long Miao , Pei-Ying Yeh
{"title":"Calcined Co-chelating, imine-crosslinking chitosan as the ORR catalyst of an anion exchange membrane fuel cell","authors":"Yen-Zen Wang ,&nbsp;Ko-Shan Ho ,&nbsp;Yu-Chang Huang ,&nbsp;Yu-Wei Cheng ,&nbsp;Chia-Long Miao ,&nbsp;Pei-Ying Yeh","doi":"10.1016/j.cartre.2024.100444","DOIUrl":null,"url":null,"abstract":"<div><div>Cobalt-chelating imine-crosslinked chitosan (Co-ICCA) is synthesized via Schiff base condensation of terephthalaldehyde and chitosan in the presence of cobalt chloride. Co-ICCA transforms into Co, N-co-doped carbon cathode catalysts (Co-N-Cs) upon calcination. The successful synthesis is confirmed using Fourier Transform Infrared Spectroscopy. The porous morphologies of the calcined Co-ICCA are characterized by transmission electron microscopy, high-resolution transmission electron microscopy, and field-emission scanning electron microscopy. The Co-N-Cs exhibit a high specific surface area (433 m²/g) and porosity, as analyzed by a BET analyzer. X-ray diffraction patterns reveal sharp graphite diffraction peaks and feature peaks of Co-crystal with an FCC lattice when the calcination temperature exceeds 800 °C, indicating high crystallinity.</div><div>Meanwhile, Raman spectra show a higher G-band intensity compared to the D-band. The performance of Co-N-Cs as cathode catalysts, particularly in the oxygen reduction reaction, is evaluated through current-voltage and linear sweep voltammetry curves and compared to commercial Pt/C catalysts. Single-cell using the Co-N-C catalyst as the cathode reaches a high maximum power density of 221 mW cm<sup>-2</sup>, close to the 285 mW cm<sup>-</sup>² achieved with Pt/C as the cathode catalyst.</div></div>","PeriodicalId":52629,"journal":{"name":"Carbon Trends","volume":"18 ","pages":"Article 100444"},"PeriodicalIF":3.1000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Trends","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667056924001238","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Cobalt-chelating imine-crosslinked chitosan (Co-ICCA) is synthesized via Schiff base condensation of terephthalaldehyde and chitosan in the presence of cobalt chloride. Co-ICCA transforms into Co, N-co-doped carbon cathode catalysts (Co-N-Cs) upon calcination. The successful synthesis is confirmed using Fourier Transform Infrared Spectroscopy. The porous morphologies of the calcined Co-ICCA are characterized by transmission electron microscopy, high-resolution transmission electron microscopy, and field-emission scanning electron microscopy. The Co-N-Cs exhibit a high specific surface area (433 m²/g) and porosity, as analyzed by a BET analyzer. X-ray diffraction patterns reveal sharp graphite diffraction peaks and feature peaks of Co-crystal with an FCC lattice when the calcination temperature exceeds 800 °C, indicating high crystallinity.
Meanwhile, Raman spectra show a higher G-band intensity compared to the D-band. The performance of Co-N-Cs as cathode catalysts, particularly in the oxygen reduction reaction, is evaluated through current-voltage and linear sweep voltammetry curves and compared to commercial Pt/C catalysts. Single-cell using the Co-N-C catalyst as the cathode reaches a high maximum power density of 221 mW cm-2, close to the 285 mW cm-² achieved with Pt/C as the cathode catalyst.
煅烧共螯合、亚胺交联壳聚糖作为阴离子交换膜燃料电池的ORR催化剂
在氯化钴的存在下,通过对苯二醛和壳聚糖的希夫碱缩合反应合成钴螯合亚胺交联壳聚糖(Co-ICCA)。Co- icca煅烧后转化为Co, n共掺杂碳阴极催化剂(Co- n - cs)。用傅里叶变换红外光谱法证实了合成的成功。通过透射电子显微镜、高分辨率透射电子显微镜和场发射扫描电子显微镜对煅烧后的Co-ICCA的多孔形貌进行了表征。通过BET分析仪分析,Co-N-Cs具有较高的比表面积(433 m²/g)和孔隙率。当煅烧温度超过800℃时,x射线衍射图显示出尖锐的石墨衍射峰和带有FCC晶格的共晶特征峰,表明结晶度较高。同时,拉曼光谱的g波段强度高于d波段。通过电流-电压和线性扫描伏安曲线评价了Co-N-Cs作为阴极催化剂的性能,特别是在氧还原反应中的性能,并与商业Pt/C催化剂进行了比较。使用Co-N-C催化剂作为阴极的单电池达到了221 mW cm-2的最高功率密度,接近Pt/C作为阴极催化剂所达到的285 mW cm-2。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Carbon Trends
Carbon Trends Materials Science-Materials Science (miscellaneous)
CiteScore
4.60
自引率
0.00%
发文量
88
审稿时长
77 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信